A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv961865



Internal ID18597111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:110581711..110612800hg38UCSC Ensembl
Innerchr2:111339288..111370377hg19UCSC Ensembl
Innerchr2:111055757..111086846hg18UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg3831090
hg1931090
hg1831090
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2198268, nssv2198269, nssv2198272, nssv2198271, nssv2198267, nssv2198266, nssv2198270, nssv2198265, nssv2198264, nssv2198263
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv961865
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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